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Haltegriff 5179

by Meyra GmbH 4 variants

Ref 292512042, 292512032, 292512082, 292512002, 292512022, 292512062, 292512052Model Rehabilitation 5179

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4032766027907A Basic UDI-DI Date18 May 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Haltegriff 5179
Model / Reference
Rehabilitation 5179, 292512042, 292512032, 292512082, 292512002, 292512022, 292512062, 292512052
Primary DI / UDI-DI
04032766027942, 04032766027935, 04032766027980, 04032766027904, 04032766027928, 04032766027966, 04032766027959
Basic UDI-DI
4032766027907A
Direct Marketing DI
04032766027904
EMDN Code
Y181806 Handles
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005780

Other devices from Meyra GmbH

See all devices from Meyra GmbH →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No